Drug recall
hCG Body Shaper, Highly Purified Human Chorionic Gonadotrophin 5000 IU, Colloidal Silver B12…
FDA recall event 76680 · Class II · Gary Wood
Key facts
| Event ID | 76680 |
|---|---|
| Recall numbers | D-0677-2017 |
| Recalling firm | Gary Wood |
| Product type | Drugs |
| Products | hCG Body Shaper, Highly Purified Human Chorionic Gonadotrophin 5000 IU, Colloidal Silver B12, Stabilizers/Excipients, Not For Medical Use, Must Be Refrigerated, Distributed by HCG Body Shaper, St… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Marketed without an Approved NDA/ANDA; FDA analysis has found the product to be tainted with human chorionic gonadotropin, rendering it an unapproved drug |
| Initiation date | Mar 28, 2017 |
| Report date | May 3, 2017 |
| Termination date | May 8, 2019 |
| City | Saint Peters |
| State | MO |
| Country | United States |
| FEI number | 3012855072 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: